REAZEAL CORP

FDA Device Registration & Listing · Wilmington, DE, US · Registration 3028271666

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3028271666
FEI Number
3028271666
Entity Name
REAZEAL CORP
City/State/Country
Wilmington, DE, US
Establishment Address
1226North King St. #485, Wilmington, DE 19801, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
REAZEAL CORP (Owner Number: 10090157)
Owner / Operator Contact Address
1226North King St. #485, Wilmington, DE 19801, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K250028
PMA Number
N/A

All Registered Proprietary Names

PRO-BOND EMERGENCY DENTURE REPAIR KIT Mouth Guard for Grinding Teeth Mouth Guard REAZEAL ANTI SNORE MOUTHPIECE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EBO Denture Repair Kit Dental Class 2 872.3570 2026-04-19
OBR Mouthguard, Over-The-Counter Unknown Class U N/A 2024-02-22
LRK Device, Anti-Snoring Dental Class 2 872.5570 2025-11-23

Official Correspondent

Fuhua Liu

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

REAZEAL CORP
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K122391 Medtronic Xomed, Inc. MEDTRONIC XOMED, INC. 2013-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3028271666. Last updated year: 2026. Please use registration number 3028271666 when referencing this establishment in official correspondence.
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